130648
4-硝基乙酰苯胺
98%
别名:
4′-硝基乙酰苯胺, 对硝基乙酰苯胺
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线性分子式:
CH3CONHC6H4NO2
化学文摘社编号:
分子量:
180.16
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
203-169-0
Beilstein/REAXYS Number:
2211962
MDL number:
Assay:
98%
产品名称
4-硝基乙酰苯胺, 98%
InChI key
NQRLPDFELNCFHW-UHFFFAOYSA-N
InChI
1S/C8H8N2O3/c1-6(11)9-7-2-4-8(5-3-7)10(12)13/h2-5H,1H3,(H,9,11)
SMILES string
CC(=O)Nc1ccc(cc1)[N+]([O-])=O
assay
98%
mp
213-215 °C (lit.)
functional group
amide
nitro
Quality Level
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Application
4-硝基乙酰苯胺可被用作检测底物，而其水解是通过UV光谱测量而确定的。它还被用于制备4-氨基乙酰苯胺。
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Hydrolysis of aromatic amides as assay for carboxylesterases-amidases.
E Heymann et al.
Methods in enzymology, 77, 405-409 (1981-01-01)
Short-column liquid chromatographic assay for caffeine and chloramphenicol in serum.
R S Markin et al.
Journal of chromatography, 525(2), 464-470 (1990-02-23)
María F Montenegro et al.
Biological chemistry, 389(4), 425-432 (2008-01-23)
Apart from its esterase activity, butyrylcholinesterase (BuChE) displays aryl acylamidase (AAA) activity able to hydrolyze o-nitroacetanilide (ONA) and its trifluoro-derivative (F-ONA). We report here that, despite amidase and esterase sites residing in the same protein, in human samples depleted of
Shinji Takenaka et al.
Journal of bioscience and bioengineering, 107(1), 27-32 (2009-01-17)
Bacillus cereus strain 10-L-2 synthesizes two arylamine N-acetyltransferases (Nat-a and Nat-b) with broad substrate specificities toward aniline and its derivatives. In southern blot analysis using probes encoding the NH2-terminus of Nat-b and a conserved region of N-acetyltransferases, digested total DNA
Dirk Volkmer et al.
Inorganic chemistry, 35(13), 3792-3803 (1996-06-19)
Dinuclear nickel(II) complexes of the ligands 2,6-bis[bis((2-benzimidazolylmethyl)amino)methyl]-p-cresol (bbapOH), N,N,N',N'-tetrakis(2-benzimidazolylmethyl)-2-hydroxy-1,3-diaminopropane (tbpOH), N-methyl-N,N',N'-tris(2-benzimidazolylmethyl)-2-hydroxy-1,3-diaminopropane (m-tbpOH) and 1-[N,N-bis(2-benzimidazolylmethyl)amino]-3-[2-(3,5-dimethyl-1H-pyrazol-1-yl)ethoxy]-2-hydroxypropane (bpepOH) were prepared in order to model the active site of urease. The novel asymmetric structures of the dinuclear complexes were characterized by X-ray structure analysis.
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